• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

粗糙脉孢菌核糖体活性的降低及稳定RNA的合成。

Reduction of ribosome activity and synthesis of stable RNA in Neurospora crassa.

作者信息

Martegani E, Popolo L, Alberghina L, Sturani E

出版信息

Biochim Biophys Acta. 1980 Dec 11;610(2):318-30. doi: 10.1016/0005-2787(80)90013-1.

DOI:10.1016/0005-2787(80)90013-1
PMID:6452164
Abstract

The addition of cycloheximide (0.02 micrograms/ml) to exponentially growing cultures of Neurospora crassa causes a reduction in growth rate and a decrease in the rate of protein accumulation, due to a partial inhibition of protein synthesis, while RNA accumulation is unaffected for about 1 h. Thus, an increased RNA:protein ratio is established in the presence of the inhibitor. RNA that accumulates during treatment with cycloheximide has the same characteristics as that of the control cultures and this, together with the enhancement of the relative rate of synthesis of ribosomal proteins induced by cycloheximide, seems to indicate that more mature ribosomes are present in cycloheximide-treated cultures. The endocellular level of several amino acids begins to increase significantly only 60 min after cycloheximide addition. A possible explanation of the stimulation of ribosome production induced by cycloheximide is given in terms of the existence of a feed-back mechanism controlling ribosome synthesis.

摘要

向指数生长的粗糙脉孢菌培养物中添加放线菌酮(0.02微克/毫升)会导致生长速率降低以及蛋白质积累速率下降,这是由于蛋白质合成受到部分抑制,而RNA积累在约1小时内不受影响。因此,在抑制剂存在的情况下会建立起增加的RNA:蛋白质比率。在用放线菌酮处理期间积累的RNA与对照培养物的RNA具有相同的特征,这一点,再加上放线菌酮诱导的核糖体蛋白质合成相对速率的提高,似乎表明在用放线菌酮处理的培养物中存在更多成熟的核糖体。仅在添加放线菌酮60分钟后,几种氨基酸的细胞内水平才开始显著增加。根据控制核糖体合成的反馈机制的存在,给出了对放线菌酮诱导核糖体产生刺激的一种可能解释。

相似文献

1
Reduction of ribosome activity and synthesis of stable RNA in Neurospora crassa.粗糙脉孢菌核糖体活性的降低及稳定RNA的合成。
Biochim Biophys Acta. 1980 Dec 11;610(2):318-30. doi: 10.1016/0005-2787(80)90013-1.
2
Multigenic control of ribosomal properties associated with cycloheximide sensitivity in Neurospora crassa.粗糙脉孢菌中与环己酰亚胺敏感性相关的核糖体特性的多基因控制。
Nature. 1974 Apr 5;248(448):508-10. doi: 10.1038/248508a0.
3
Early response and induced tolerance to cycloheximide in Neurospora crassa.粗糙脉孢菌对放线菌酮的早期反应和诱导耐受性。
Curr Genet. 1989 Jun;15(6):429-34. doi: 10.1007/BF00376800.
4
Biochemical genetic studies of cycloheximide resistance in Neurospora crassa.粗糙脉孢菌中放线菌酮抗性的生化遗传学研究。
Biochem Genet. 1975 Jun;13(5-6):283-300. doi: 10.1007/BF00485814.
5
Intracellular protein degradation in Neurospora crassa.
J Biol Chem. 1979 Aug 10;254(15):7047-54.
6
Structure of the translating ribosome arrested by cycloheximide.环己酰亚胺抑制的翻译核糖体的结构。
Proc Natl Acad Sci U S A. 2021 Nov 30;118(48). doi: 10.1073/pnas.2111862118.
7
3-Amino-1,2,4-triazole is an inhibitor of protein synthesis on mitoribosomes in Neurospora crassa.3-氨基-1,2,4-三唑是粗糙脉孢菌中线粒体核糖体上蛋白质合成的抑制剂。
Biochim Biophys Acta. 1980 Apr 30;607(2):339-49. doi: 10.1016/0005-2787(80)90086-6.
8
On the role of protein synthesis in the circadian clock of Neurospora crassa.蛋白质合成在粗糙脉孢菌生物钟中的作用
Proc Natl Acad Sci U S A. 1988 Feb;85(4):1096-100. doi: 10.1073/pnas.85.4.1096.
9
Role of ribosomes in cycloheximide resistance of Neurospora mutants.核糖体在粗糙脉孢菌突变体对放线菌酮抗性中的作用。
Mol Gen Genet. 1973 Aug 28;124(4):359-63. doi: 10.1007/BF00267664.
10
Cycloheximide-induced phase shifting of circadian clock of Neurospora.环己酰亚胺诱导的粗糙脉孢菌生物钟相位移动
Am J Physiol. 1981 Jul;241(1):R31-5. doi: 10.1152/ajpregu.1981.241.1.R31.

引用本文的文献

1
TBX2 expression is regulated by PAX3 in the melanocyte lineage.TBX2 的表达受 PAX3 在黑素细胞谱系中的调控。
Pigment Cell Melanoma Res. 2013 Jan;26(1):67-77. doi: 10.1111/pcmr.12029. Epub 2012 Nov 21.
2
Control of growth and of the nuclear division cycle in Neurospora crassa.粗糙脉孢菌生长与核分裂周期的调控
Microbiol Rev. 1981 Mar;45(1):99-122. doi: 10.1128/mr.45.1.99-122.1981.